The International C. elegans Conference takes place every two years and features cutting-edge research in a diverse array of topics, including physiology, neurobiology, development, evolution, behavior, aging, ecology, gene regulation, genomics, and more. For 2021, #Worm21 has been reimagined for a virtual platform and will focus on early career researchers at every stage.
We’re happy to confirm the next webinar in our Development presents… series will be chaired by our Editor Swathi Arur (The University of Texas MD Anderson Cancer Center), who has brought together talks that span her interests in C. elegans development, the germline and cell signalling.
The webinar will be held in Remo, our browser-based conferencing platform – after the talks you’ll have the chance to meet the speakers and other participants at virtual conference tables. If you can’t make it on the day, talks will be available to watch for a couple of weeks after the event (look out for details on the Node).
For more information about what to expect in Remo, go to
Updated 11 January. Let us know if we missed anything
Various organisations and looser assemblies of locked down researchers have begun to put together online seminar and talk series, many of which are open to anyone (usually with registration), and many of which also have previous talks recorded.
Here’s a list of what we’ve found recently, developmental biology and adjacent – please let us know if we missed anything so we can keep it up to date. For upcoming virtual developmental biology conferences/symposia, see our Events calendar page.
First up from us is Development presents…, the webinar series hosted each month by a different Development Editor which will be a platform for early career researchers to share their work. As well as the talks, you also have the chance to meet the speakers and other participants at interactive video tables – giving the developmental biology community the chance to network virtually.
The next webinar will be Wednesday 13 January, 16.00 GMT, hosted by Swathi Arur and featuring talks from Brandon Scott Carpenter, Hayao Ohno and Swann Floc’hlay.
Next talk: January 14, Evolutionary Studies:
Just Under the Surface: Leveraging Zebrafish to Understand the Interplay Between Evolution and Development
We currently have an opening for a Reviews Editor as a maternity cover position on Development. As this is a temporary position, we are specifically looking for candidates with editorial experience.
Core responsibilities of the position include:
Commissioning, handling peer review and developmental editing of material for the front section of the journal
Representing the journal at international conferences and within the wider scientific community
Writing press releases, article highlights and material for Development’s community website ‘the Node’
Creative involvement in the journal’s development
For further details and instructions on how to apply, please see the full job advert here. If you are interested in applying, but would like further information or have any questions, please feel free to drop me an email.
Naa12 rescues embryonic lethality in Naa10-Deficient Mice in the amino-terminal acetylation pathway
Hyae Yon Kweon, Mi-Ni Lee, Max Dörfel, Seungwoon Seo, Leah Gottlieb, Thomas Papazyan, Nina McTiernan, Rasmus Ree, Andrew Garcia, Michael Flory, Jonathan Crain, Alison Sebold, Scott Lyons, Ahmed Ismail, Elaine Marchi, Seong-keun Sonn, Se-Jin Jeong, Sejin Jeon, Shinyeong Ju, Simon J. Conway, TaeSoo Kim, Hyun-Seok Kim, Cheolju Lee, Tae-Young Roh, Thomas Arnesen, Ronen Marmorstein, Gholson J. Lyon, Goo Taeg Oh
Serine Palmitoyltransferase Controls Stemness of Intestinal Progenitors
Ying Li, Bhagirath Chaurasia, Vincent Kaddai, Joseph L. Wilkerson, J. Alan Maschek, James Cox, Peng Wei, Claire Bensard, Peter J Meikle, Hans Clevers, James A Shayman, Yoshio Hirabayashi, William L. Holland, Jared Rutter, Scott A. Summers
CTCF is a Barrier for Totipotent-like Reprogramming
Teresa Olbrich, Maria Vega-Sendino, Desiree Tillo, Wei Wu, Nicholas Zolnerowich, Andy D. Tran, Catherine N. Domingo, Mariajose Franco, Marta Markiewicz-Potoczny, Gianluca Pegoraro, Peter C. FitzGerald, Michael J. Kruhlak, Eros Lazzerini-Denchi, Elphege P. Nora, Andre Nussenzweig, Sergio Ruiz
Robust integrated intracellular organization of the human iPS cell: where, how much, and how variable?
Matheus P. Viana, Jianxu Chen, Theo A. Knijnenburg, Ritvik Vasan, Calysta Yan, Joy E. Arakaki, Matte Bailey, Ben Berry, Antoine Borensztejn, Jackson M. Brown, Sara Carlson, Julie A. Cass, Basudev Chaudhuri, Kimberly R. Cordes Metzler, Mackenzie E. Coston, Zach J. Crabtree, Steve Davidson, Colette M. DeLizo, Shailja Dhaka, Stephanie Q. Dinh, Thao P. Do, Justin Domingus, Rory M. Donovan-Maiye, Tyler J. Foster, Christopher L. Frick, Griffin Fujioka, Margaret A. Fuqua, Jamie L. Gehring, Kaytlyn A. Gerbin, Tanya Grancharova, Benjamin W. Gregor, Lisa Harrylock, Amanda Haupt, Melissa C. Hendershott, Caroline Hookway, Alan R. Horwitz, Chris Hughes, Eric J. Isaac, Gregory R. Johnson, Brian Kim, Andrew N. Leonard, Winnie Leung, Jordan J. Lucas, Susan A. Ludmann, Blair M. Lyons, Haseeb Malik, Ryan McGregor, Gabe E. Medrash, Sean L. Meharry, Kevin Mitcham, Irina A. Mueller, Timothy L. Murphy-Stevens, Aditya Nath, Angelique M. Nelson, Luana Paleologu, T. Alexander Popiel, Megan M. Riel-Mehan, Brock Roberts, Lisa M. Schaefbauer, Magdalena Schwarzl, Jamie Sherman, Sylvain Slaton, M. Filip Sluzewski, Jacqueline E. Smith, Youngmee Sul, Madison J. Swain-Bowden, W. Joyce Tang, Derek J. Thirstrup, Daniel T. Toloudis, Andrew P. Tucker, Veronica Valencia, Winfried Wiegraebe, Thushara Wijeratna, Ruian Yang, Rebecca J. Zaunbrecher, Allen Institute for Cell Science, Graham T. Johnson, Ruwanthi N. Gunawardane, Nathalie Gaudreault, Julie A. Theriot, Susanne M. Rafelski
Dog color patterns explained by modular promoters of ancient canid origin
Danika L. Bannasch, Christopher B. Kaelin, Anna Letko, Robert Loechel, Petra Hug, Vidhya Jagannathan, Jan Henkel, Petra Roosje, Marjo K. Hytönen, Hannes Lohi, Meharji Arumilli, DoGA consortium, Katie M. Minor, James R. Mickelson, Cord Drögemüller, Gregory S. Barsh, Tosso Leeb
Molecular topography of an entire nervous system
Seth R Taylor, Gabriel Santpere, Alexis Weinreb, Alec Barrett, Molly B. Reilly, Chuan Xu, Erdem Varol, Panos Oikonomou, Lori Glenwinkel, Rebecca McWhirter, Abigail Poff, Manasa Basavaraju, Ibnul Rafi, Eviatar Yemini, Steven J Cook, Alexander Abrams, Berta Vidal, Cyril Cros, Saeed Tavazoie, Nenad Sestan, Marc Hammarlund, Oliver Hobert, David M. Miller III
Automated hiPSC culture and sample preparation for 3D live cell microscopy
Mackenzie E. Coston, Benjamin W. Gregor, Joy Arakaki, Antoine Borensztejn, Thao P. Do, Margaret A. Fuqua, Amanda Haupt, Melissa C. Hendershott, Winnie Leung, Irina A. Mueller, Angelique M. Nelson, Susanne M. Rafelski, Madison J. Swain-Bowden, W. Joyce Tang, Derek J. Thirstrup, Winfried Wiegraebe, Calysta Yan, Ruwanthi N Gunawardane, Nathalie Gaudreault
Scalable production of tissue-like vascularised liver organoids from human PSCs
Sean P Harrison, Richard Siller, Yoshiaki Tanaka, Yangfei Xiang, Benjamin Patterson, Henning Kempf, Espen Melum, Kathrine S Åsrud, Maria E Chollet, Elisabeth Andersen, Per Morten Sandset, Saphira Baumgarten, Flavio Bonanini, Dorota Kurek, Santosh Mathapati, Runar Almaas, Kulbhushan Sharma, Steven R Wilson, Frøydis S Skottvoll, Ida C Boger, Inger L Bogen, Tuula A Nyman, Jun J Wu, Ales Bezrouk, Dana Cizkova, Jaroslav Mokry, Robert Zweigerdt, In-Hyun Park, Gareth J Sullivan
We live in an ageing society with high incidence of cognitive, sensory and motor decline, as well as neurodegenerative diseases such as Alzheimer’s disease (AD) or Fronto-temporal Dementia (FTD). Although decay of synaptic functions is a clear hallmark of the aforementioned conditions, we know too little about the underlying causes. The overarching aim of this project is to study roles of the ageing- and neurodegenerative disease-related factor Tau during the regulation of synapses in health, ageing and disease.
Synapses are specialised neuronal cell junctions which contain complex machinery for rapid transmission of signals to partner cells. This machinery is frequently disrupted during ageing and in neurodegeneration and the resulting synaptic malfunction is an important cause for cognitive, sensory and motor decline. The underpinning mechanisms are poorly understood. To bridge this knowledge gap, we focus on Tau. Tau plays a vital role in the pathogenesis of neurodegenerative disorders and is also linked to physiological ageing. Accordingly, Tau is an important therapeutic target for the development of treatments of AD and FTD.
Considering Tau’s crucial roles during pathogenesis and treatment of dementia, it is vital to understand its physiological function. Tau loss is known to lead to age-related synaptic deficits both in mice and the fruit fly Drosophila, and our work has started to deliver first explanations. Thus, we have shown that Tau loss triggers aberrations of microtubule networks and axonal transport deficits affecting synapse formation and maintenance (Voelzmann et al., 2016, eLife 5, e14694ff.; Hahn et al., 2020, bioRxiv 2020.08.19.257808ff.). We now find from our proteomic and preliminary functional studies that Tau plays even more direct roles by binding to factors that are important for synaptic function. The aim of this project is to understand these synaptic mechanisms of Tau. For this, we will use the model organism Drosophila which harbours Tau and synaptic machinery that is well conserved with humans, but can be studied far more effectively than in other model organisms. Using Drosophila‘s efficient genetics, powerful experimental strategies and simple robust behavioural assays, you will study the functional links between Tau and its synaptic binding partners. This will involve inter-disciplinary approaches using genetics, molecular biology, biochemistry, cell biology, cell culture and in vivo studies, cutting-edge bioimaging of synaptic activity and behavioural studies. You will unravel mechanisms of Tau at synapses as a means to understand neuronal decay during ageing and in neurodegeneration.
Applications from candidates, ideally with some background in cell biology, genetics, neuroscience and/or biomedical sciences are encouraged to apply. The successful applicant will be based in the Institute of Systems, Molecular & Integrative Biology, University of Liverpool, supervised by Dr Sánchez-Soriano (https://sanchezlab.wordpress.com/research/), whilst working closely with Dr Olena Riabinina (http://insectneurolab.com/) at the Department of Biosciences, Durham University. Interested applicants should contact Dr Sanchez-Soriano to discuss the project: n.sanchez-soriano@liverpool.ac.uk.
A postdoctoral research associate position is available immediately to investigate the role of reactive oxygen species (ROS) as physiological signaling molecules in axonal growth and guidance in the lab of Dr. Daniel M. Suter at Purdue University, West Lafayette, IN https://suterlab.bio.purdue.edu/. Specifically, the work will investigate the molecular and cellular mechanisms of how ROS regulate axonal growth and guidance in vitro and in vivo. The successful applicant has experience in cell biology and molecular biology. Additional expertise in developmental neuroscience, microscopy, and working with zebrafish is desirable but not required. This position is supported through funding from the NIH.
Highly motivated candidates with a PhD in cell biology, molecular biology, or neuroscience who are interested to participate in this exciting project at the interface of cellular and developmental neurobiology are invited to send their CV, a brief statement of research interests and contact information of three referees to Dr. Suter.
Dr. Daniel M. Suter
Department of Biological Sciences
Purdue University
915 West State Street
West Lafayette, IN 47907
USA dsuter@purdue.edu
765-496-1562
The BiOf lab http://biof-lab.org/ has developed a microfluidic technique, the Cellular Capsules Technology, that allows them to produce multicellular spheroids and organoids in a high throughput and controlled format. The applications in tissue engineering, oncology and regenerative medicine and toxicology testing are numerous. The recruited postdocs will be involved in the interdisciplinary projects pursued by the team in engineering multiscale vascularized tissues, reconstructing a functional liver lobule, deciphering the impact of mechanical cues on hepatocarcinoma and glioblastoma progression in vitro models, developing innovative microscopy techniques for thick tissue imaging.
We seek for talented scientists with exceptional motivation and outstanding expertise (i.e. PhD) in biophotonics /image analysis, cancer or stem cell biology, microfluidics, biophysics or tissue engineering.
The proposed funding is for 12 months and can be renewed up to 36 months. The salary will be adapted to the experience of the applicant. Starting date will be between March and June 2021.
A postdoctoral research position is available in the group of Dr. Kristen Panfilio at the University of Warwick, UK, to join our BBSRC-funded project on how polyploid nuclear structure influences cellular function in dynamic epithelial tissues. This is a full-time, fixed-term position for up to 36 months, integrating developmental biology, bioinformatics, cell cycle regulation, genome organization, and 4D live cell imaging.
Polyploidy is hypothesized to aid epithelial barrier formation and its repair after wounding and to rapidly supply gene products by transcription from multiple gene copies. Yet polyploid genomic structure may be unstable and require active inhibition of apoptosis through regulatory processes that are not yet well understood. Investigating the costs and benefits of polyploidy is essential to understand tissue-specific development, homeostasis, and ageing.
The two extraembryonic tissues of insects offer an excellent – and inherently comparative – research model, spanning key developmental stages for morphogenesis and cellular physiology. Our research species is the flour beetle Tribolium castaneum, which offers advanced genetic resources and where we integrate fluorescent live cell imaging and next-generation sequencing approaches (see the lab’s recent publications in eLife 5:e13834, Development 143:3002, Commun. Biol. 3:552). The project uses methods to assess nuclear size and tissue integrity, quantify gene expression, and genetically challenge barrier organization and cell number. Altogether, we will test long-standing hypotheses on polyploidy function and its end-stage implications in animal tissues. A complete description of the project is available at: https://gtr.ukri.org/projects?ref=BB%2FV002392%2F1.
You will have a Ph.D. or equivalent and good knowledge and experience in genetics, cell and developmental biology, standard molecular biology techniques,and working with NGS data, as evidenced by your Ph.D. thesis and/or authored papers in peer-reviewed journals. Familiarity with the fields of insect developmental genetics and comparative genomics would also be highly advantageous. Practical experience in any of the following is desired: advanced microscopy (including light sheet fluorescence microscopy),RNAi, FACS, RT-qPCR, and computational work with either sequencing or imaging data. We will provide full training in new techniques, supported by the possibility for international travel and collaboration.
Enquiries and expressions of interest directly to Kristen (K.Panfilio@warwick.ac.uk) are welcome, with applications made on-line (post number 103508). Full applications will include contact details for at least two referees, a CV, and covering letter stating why you are interested in the topic and what you would bring to the project. The application closing date is 7th February 2021.
The patterning of stomata – the pores in the plant epidermis that facilitate gas exchange and water control – is regulated by a family of small secreted peptides. A new paper in Development analyses the effective ranges of two such peptides, borrowing a statistical technique used by astrophysicists to investigate the distribution and patterning of galaxies. We caught up with authors Emily Lo, who worked on the project when an undergraduate at the University of Washington (UW), and her supervisor Keiko Torii, who recently moved her lab from UW to The University of Texas at Austin (where she is Professor and Johnson & Johnson Centennial Chair in Plant Cell Biology), to hear more about the story.
Emily (L) and Keiko (R)
Keiko, can you give us your scientific biography and the questions your lab is trying to answer?
KT: As a plant developmental biologist, I was always super fascinated by how dazzling arrays of functional, beautiful patterns emerge during development and how the external environment, where plants thrive, shapes the manifestation of such functional patterns. My main focus is to tackle such observations through understanding the molecular and genetic basis of cell-cell communication, ‘how plant cells talk to each other to generate functional patterns’.
I received my PhD and did my first short postdoc in Japan, where I identified the causal gene for the Arabidopsis mutant, erecta, which exhibits short stature and altered organ shape. It turned out that the ERECTA gene encodes a putative receptor kinase (collectively known as ‘Receptor-like Kinase’ or ‘RLK’), and it was the first report that this type of putative peptide receptor regulates plant growth and development. Later, after I obtained a tenure-track Assistant Professor position at the UW in Seattle, our research elucidated that ERECTA-family RLKs perceive a family of peptides to enforce proper stomatal patterning, which is the basis of this work.
In the Fall of 2019, I accepted the Johnson & Johnson Centennial Chair in Plant Cell Biology at the Department of Molecular Biosciences, The University of Texas at Austin. Currently I am also a Howard Hughes Medical Investigator.
And Emily – how did you come to work in Keiko’s lab on this project?
EL: I was lucky enough to be hired as an undergrad in Keiko’s lab during my freshman year at UW, and I stayed on until I graduated. It’s a rare opportunity to have such a long research experience as an undergrad, so I was able to devote a substantial amount of time to this project. Keiko introduced me to this fascinating project using mosaic fluorescent sectors to track peptide expression, which had been initiated by Dr. Takeshi Kuroha, a previous postdoctoral fellow, and Janelle Sagawa, a previous undergrad researcher (both acknowledged in the manuscript). So right away I could start growing seedlings, generating these mosaic sectors, and imaging on the confocal microscope. It was great fun! I graduated before we were able to complete the project, so Scott [Zeng] developed the majority of the SPACE pipeline after I left the lab.
How has your research been affected by the COVID-19 pandemic?
KT: Unfortunately, my lab and research program got hit really hard by the COVID-19 situation, because we had just relocated from Seattle WA to Austin TX right before the pandemic hit. Our brand-new lab at UT Austin was finally operating in the beginning of 2020 when we had to suddenly shut it down. Like myself, almost all the new lab members were new to Texas (or the Southern part of USA), and many were separated from family. So, staying at home in an unfamiliar city was stressful to everyone, and I truly thank my lab members for being positive and hanging together during this exceptionally difficult time. As for this manuscript, since we were at the phase of drafting a manuscript (lucky us!), Scott and I completed the manuscript during the full shut down phase, with thoughtful inputs from Emily and other co-authors. New online technology, such as Zoom, helped us work together, remotely.
EL: For this project, it was fortunate in that all experiments were completed and we were at the data analysis phase before COVID hit, so we were able to complete it through online communication (and because I’m located in Baltimore, I’d been communicating solely online anyway). For my current research at Hopkins, we were in an Essential-Only phase from March to June, in which no new experiments were allowed to begin; luckily, at that point I did have some computational analysis to catch up on. In mid-June we had our Phase-I reopening, so I’ve been able to resume many of my experiments, though of course progress is still limited by how much time we’re allotted in the lab.
Why have the signalling ranges of peptides like EPF1 and Stomagen been hard to assess, prior to your paper?
EL & KT: Whether secreted peptides or small chemical hormones, how far the signal moves is a fundamental question of pattern formation in development. But precisely quantifying the distance is not trivial. For direct observation, one could tag fluorescent proteins (or exogenously synthesize a peptide conjugated with a fluorophore). In a strict sense, however, such modifications change the size and property of peptides or chemical signals. Alternatively, one could develop sensors (such as a FRET sensor) that detect the existence of peptides or chemical signals.
We have previously shown that EPIDERMAL PATTERNING FACTOR (EPF) family members of secreted peptides fine-tune patterning of stomata on the plant epidermis by competitive binding to the same receptor. Because of the flat, two-dimensional nature of the developing leaf epidermis, we thought that our system would be a great model for understanding how far the secreted peptides influence tissue patterning, rather than directly observing its movement.
Can you give us the key results of the paper in a paragraph?
EL & KT: Using recombination-based mosaic sectors to overexpress signaling peptides EPF1 and Stomagen, which inhibit and promote stomatal development, respectively, we determined the effective ranges of these peptides in Arabidopsis cotyledons. We developed a quantitative pipeline to model stomatal distributions across the cotyledon in response to peptide overexpression, which we named SPACE (stomata patterning autocorrelation on epidermis), an homage to the astrophysics origin of the autocorrelation approach. We found that the inhibitor peptide EPF1 has a longer effective range than the activator peptide STOMAGEN, and that the patterning effects of peptide overexpression are limited to a local range rather than the global cotyledon.
Tile scan of Arabidopsis thaliana cotyledon with mosaic sectors simultaneously overexpressing GFP, retained in the endoplasmic reticulum, and secreted peptide EPF1, an inhibitor of stomatal differentiation.
How did you come upon the idea of borrowing an astrophysical technique to look at stomatal patterning?
KT: At the initial stage of our research, we were able to produce chimeras via heat-shock Cre/lox recombination, but we could not think of how to actually ‘calculate’ the effective distance of the peptides. Initially, we tried to set bin range (such as 100 μm, 200 μm, etc.) from each sector border. However, because of the complex geometry of pavement cells as well as the unique size, shape and location of individual sectors, we could not figure out how to normalize stomatal distribution surrounding each sector.
One morning in the kitchen, I was talking about this problem to my spouse, who is a theoretical physicist studying String Theory. When I was drawing a cartoon of a simple leaf (essentially an oval) with lots of stomata (essentially dots inside the oval), he told me, ‘this sounds familiar to me. I think my colleague, Miguel, is addressing the exact same problem – except that in his case, it’s the distribution of galaxies in the Universe’. I immediately e-mailed Prof. Miguel Morales of UW Physics. I thought that he might think I was crazy, but to my pleasant surprise, Miguel and his postdoc Dr Bryna Hazelton were very excited to hear about our research and the potential of the spatial autocorrelation statistics that they utilize for astrophysics in solving questions in plant development. Bryna mentored Emily in programming for the spatial autocorrelation analysis.
My Physics colleagues generously gave me the opportunity to give a 15 min talk to incoming Physics Graduate Students. I discussed the principles of spatial patterning in biological systems and introduced Alan Turing’s reaction-diffusion model; luckily, Scott remembered my brief talk and was curious enough to join my lab to tackle this problem after Emily’s graduation.
EL: For me it started when Keiko suggested we meet with Miguel and Bryna. When we explained that we were trying to generate a metric of epidermal spatial patterning, they almost immediately suggested looking into autocorrelation, an astrophysics method for analyzing galaxy distributions/patterning. Bryna works at the UW eScience Institute, and has a goal to empower the next generation of researchers and students to answer fundamental questions in complex or noisy data. Working with her to develop code to analyze our epidermal patterning questions was a really wonderful and fruitful experience, and that was the starting point for our collaboration and the development of the SPACE pipeline.
Why do you think the stomatal inhibitor EPF1 is able to travel farther than the activator Stomagen?
EL & KT: To clarify your question, the goal of our study was to determine how far these peptides act or have an effect, not necessarily the physical distance they travel. EPF1 has a longer range in terms of developmental outcome than Stomagen, but not necessarily diffusion distance. The question of their differing ranges is complex because stomatal lineage cells (which are induced by Stomagen) will themselves secrete EPF1, acting as a negative-feedback loop; in other words, the peptides are not acting in isolation. Our quantitative determination of peptide effective range is fascinating because in the Turing theory of pattern formation, a short-range activator often interacts with a longer-range inhibitor to achieve a self-regulating, periodic pattern. The relationship between Stomagen and EPF1 might be one such example of this effect to achieve regular, ordered stomatal spacing across the epidermis.
When doing the research, did you have any particular result or eureka moment that has stuck with you?
EL: After we’d established that the mosaic sector generation system indeed worked, we wanted to observe the potential global effects of peptide overexpression (from within the restricted mosaic sectors) across the entire cotyledon, so I switched to a confocal microscope that had tile-scanning functionality. The stitched image I got of the entire cotyledon surface was very beautiful; getting that first image was a hugely satisfying and validating moment for me.
Getting that first image was a hugely satisfying and validating moment for me
And what about the flipside: any moments of frustration or despair?
EL: The initial months were the most difficult experimentally for me. There were a lot of experimental skills that required finesse, for example sowing tiny Arabidopsis seeds individually on plates or mounting the cotyledons on glass slides completely flat without folding or tearing, etc. The way I overcame these challenges was practice and repetition: those are just skills that are gained slowly over time.
I understand you’ve now left Keiko’s lab – what are you doing now?
EL: I’m currently pursuing my PhD in Biomedical Engineering at Johns Hopkins, in the labs of Prof. Patrick Cahan and Prof. Andrew Feinberg. I study how changes in cell identity relate to cancer initiation in the context of pancreatic ductal adenocarcinoma: one of the most lethal malignancies in the US.
Even though I work on human disease research now, plant research is still very important to me, especially given the adaptations humans will have to make to agricultural practices in response to global climate change. Particularly, I think optimizing crop water consumption will be a key strategy in the next several decades to reach necessary agricultural yields in fluctuating environmental conditions.
Where will this story take the Torii lab?
KT: Stomatal patterning and distribution is critical for plant productivity and water use efficiency, and many different genetic and environmental factors (such as temperature, light, CO2 and drought) influence stomatal number, density and distribution. There is a long history in Plant Physiology of studying these traits. Yet, essentially, there are two ways to quantify these traits: stomata density (number of stomata per given area) and stomatal index (number of stomata per total epidermal cells). Different genetic backgrounds and environmental conditions may influence number, density or distribution in unique ways, but often such information is lost by simply presenting bar graphs of stomatal density and index. So, the natural next direction is to apply SPACE pipelines to describe different patterns of stomata, in different ages of Arabidopsis leaves or under different genetic/environmental conditions. Further harnessing the SPACE pipeline to quantitatively characterize stomatal patterning of agronomically important plant species, such as tomato and cereals, may reveal some important characteristics. Finally, we are looking for developmental biologists studying pattern formation of any systems who are brave enough to try out our SPACE pipeline to quantitatively characterize their systems.
Finally, let’s move outside the lab – what do you like to do in your spare time in Baltimore and Austin?
KT: Well…since I just relocated alone to a small one-bedroom apartment in Austin, and then the COVID-19 stay-at-home order was put in place, I really did not have much time to explore my new city. My spouse and children were supposed to move to Austin from Seattle this summer, but this got postponed due to COVID-19. I really hope that, when we (the USA) manage to get the pandemic under control, I can explore the Texas Hill Country and enjoy its natural beauty, and see bluebonnet wildflowers blooming for the first time in my life!
EL: I’m an avid baker, cook and gardener. During COVID-19, I’ve boarded the sourdough starter bandwagon as an at-home quarantine activity. And as much as possible, I’ve tried to stay in touch with friends and family across the country and the world by video chatting.